Superroot, a recessive mutation in Arabidopsis, confers auxin overproduction.

We have isolated seven allelic recessive Arabidopsis mutants, designated superroot (sur1-1 to sur1-7), displaying several abnormalities reminiscent of auxin effects. These characteristics include small and epinastic cotyledons, an elongated hypocotyl in which the connection between the stele and cortical and epidermal cells disintegrates, the development of excess adventitious and lateral roots, a reduced number of leaves, and the absence of an inflorescence. When germinated in the dark, sur1 mutants did not develop the apical hook characteristic of etiolated seedlings. We were able to phenocopy the Sur1- phenotype by supplying auxin to wild-type seedlings, to propagate sur1 explants on phytohormone-deficient medium, and to regenerate shoots from these explants by the addition of cytokinins alone to the culture medium. Analysis by gas chromatography coupled to mass spectrometry indicated increased levels of both free and conjugated indole-3-acetic acid. sur1 was crossed to the mutant axr2 and the altered-auxin response mutant ctr1. The phenotype of both double mutants was additive. The sur1 gene was mapped on chromosome 2 at 0.5 centimorgans from the gene encoding phytochrome B.

[1]  J. Slovin,et al.  Rethinking Auxin Biosynthesis and Metabolism , 1995, Plant physiology.

[2]  M. Estelle,et al.  The axr2-1 mutation of Arabidopsis thaliana is a gain-of-function mutation that disrupts an early step in auxin response. , 1994, Genetics.

[3]  K. Szczyglowski,et al.  iaglu, a gene from Zea mays involved in conjugation of growth hormone indole-3-acetic acid. , 1994, Science.

[4]  C. Maurel,et al.  Alterations of Auxin Perception in rolB-Transformed Tobacco Protoplasts (Time Course of rolB mRNA Expression and Increase in Auxin Sensitivity Reveal Multiple Control by Auxin) , 1994, Plant physiology.

[5]  G. Fink,et al.  Differential regulation of an auxin-producing nitrilase gene family in Arabidopsis thaliana. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[6]  E. Weiler,et al.  Molecular characterization of two cloned nitrilases from Arabidopsis thaliana: key enzymes in biosynthesis of the plant hormone indole-3-acetic acid. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[7]  C. Maurel,et al.  The rolB Gene of Agrobacterium rhizogenes Does Not Increase the Auxin Sensitivity of Tobacco Protoplasts by Modifying the Intracellular Auxin Concentration , 1994, Plant physiology.

[8]  M. Estelle,et al.  Genetic approaches to auxin action. , 1994, Plant, cell & environment.

[9]  P. Green,et al.  Characterization of the Auxin-Inducible SAUR-AC1 Gene for Use as a Molecular Genetic Tool in Arabidopsis , 1994, Plant physiology.

[10]  G. Fink,et al.  Arabidopsis thaliana auxotrophs reveal a tryptophan-independent biosynthetic pathway for indole-3-acetic acid. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[11]  F. Ausubel,et al.  A procedure for mapping Arabidopsis mutations using co-dominant ecotype-specific PCR-based markers. , 1993, The Plant journal : for cell and molecular biology.

[12]  Candace Timpte,et al.  Arabidopsis auxin-resistance gene AXR1 encodes a protein related to ubiquitin-activating enzyme E1 , 1993, Nature.

[13]  T. Schmülling,et al.  Indole-3-acetic acid homeostasis in transgenic tobacco plants expressing the Agrobacterium rhizogenes rolB gene , 1993 .

[14]  T. Schmülling,et al.  Hormonal content and sensitivity of transgenic tobacco and potato plants expressing single rol genes of Agrobacterium rhizogenes T‐DNA , 1993 .

[15]  Joseph R. Ecker,et al.  CTR1, a negative regulator of the ethylene response pathway in arabidopsis, encodes a member of the Raf family of protein kinases , 1993, Cell.

[16]  J. Chory,et al.  Mutations in the gene for the red/far-red light receptor phytochrome B alter cell elongation and physiological responses throughout Arabidopsis development. , 1993, The Plant cell.

[17]  H. Klee,et al.  Uncoupling Auxin and Ethylene Effects in Transgenic Tobacco and Arabidopsis Plants. , 1993, The Plant cell.

[18]  B. Sundberg,et al.  Conjugation of Indole-3-Acetic Acid (IAA) in Wild-Type and IAA-Overprodcing Transgenic Tobacco Plants, and Identification of the Main Conjugates by Frit-Fast Atom Bombardment Liquid Chromatography-Mass Spectrometry , 1993, Plant physiology.

[19]  B. Sotta,et al.  Enhancement of Naphthaleneacetic Acid-Induced Rhizogenesis in T(L)-DNA-Transformed Brassica napus without Significant Modification of Auxin Levels and Auxin Sensitivity. , 1992, Plant physiology.

[20]  A. Ortuño,et al.  The decrease in auxin polar transport down the lupin hypocotyl could produce the indole-3-acetic Acid distribution responsible for the elongation growth pattern. , 1992, Plant physiology.

[21]  J. Verdeil,et al.  Oil palm (Elaeis guineensis Jacq.) clonal fidelity : endogenous cytokinins and indoleacetic acid in embryogenic callus cultures , 1992 .

[22]  B. Sundberg,et al.  Transgenic Tobacco Plants Coexpressing the Agrobacterium tumefaciens iaaM and iaaH Genes Display Altered Growth and Indoleacetic Acid Metabolism. , 1992, Plant physiology.

[23]  M. Van Montagu,et al.  Molecular genetic approaches to plant development. , 1992, The International journal of developmental biology.

[24]  J. Slovin,et al.  Indole-3-Acetic Acid Biosynthesis in the Mutant Maize orange pericarp, a Tryptophan Auxotroph , 1991, Science.

[25]  C. Bell,et al.  Requirement of the Auxin Polar Transport System in Early Stages of Arabidopsis Floral Bud Formation. , 1991, The Plant cell.

[26]  J. Suttle Biochemical Bases for the Loss of Basipetal IAA Transport with Advancing Physiological Age in Etiolated Helianthus Hypocotyls: Changes in IAA Movement, Net IAA Uptake, and Phytotropin Binding. , 1991, Plant physiology.

[27]  J. Brusslan,et al.  Phytochrome control of the tms2 gene in transgenic Arabidopsis: a strategy for selecting mutants in the signal transduction pathway. , 1991, The Plant cell.

[28]  J. Slovin,et al.  Stable Isotope Labeling, in Vivo, of d- and l-Tryptophan Pools in Lemna gibba and the Low Incorporation of Label into Indole-3-Acetic Acid. , 1991, Plant physiology.

[29]  H. Klee,et al.  Inactivation of auxin in tobacco transformed with the indoleacetic acid-lysine synthetase gene of Pseudomonas savastanoi. , 1991, Genes & development.

[30]  B. Sundberg,et al.  Free and Conjugated Indoleacetic Acid (IAA) Contents in Transgenic Tobacco Plants Expressing the iaaM and iaaH IAA Biosynthesis Genes from Agrobacterium tumefaciens. , 1991, Plant physiology.

[31]  Bath Ba,et al.  The role of endogenous auxin in root initiation Part I .•Evidence from studies on auxin application, and analysis of endogenous levels , 1991 .

[32]  A. Ortuño,et al.  Changes in the concentration of indole‐3‐acetic acid during the growth of etiolated lupin hypocotyls , 1990 .

[33]  M. Freeling Patterns in plant development (2nd edn) , 1990 .

[34]  F. Ausubel,et al.  Arabidopsis thaliana mutant that develops as a light-grown plant in the absence of light , 1989, Cell.

[35]  J. Cohen,et al.  Quantitation of indoleacetic Acid conjugates in bean seeds by direct tissue hydrolysis. , 1989, Plant physiology.

[36]  M. Van Montagu,et al.  Agrobacterium tumefaciens-mediated transformation of Arabidopsis thaliana root explants by using kanamycin selection. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[37]  J. Cohen,et al.  Levels of Indole-3-Acetic Acid in Lemna gibba G-3 and in a Large Lemna Mutant Regenerated from Tissue Culture. , 1988, Plant physiology.

[38]  Peter J. Davies,et al.  Plant Hormones and their Role in Plant Growth and Development , 1987, Springer Netherlands.

[39]  H. Klee,et al.  The effects of overproduction of two Agrobacterium tumefaciens T-DNA auxin biosynthetic gene products in transgen c petunia plants , 1987 .

[40]  M. Koornneef,et al.  Procedures for mapping by using F2 and F3 populations. , 1987 .

[41]  A. Ortuño,et al.  Distribution of indole‐3‐acetic acid in relation to the growth of etiolated Lupinus albus hypocotyls , 1986 .

[42]  J. Slovin,et al.  C(6)-[benzene ring]-indole-3-acetic Acid: a new internal standard for quantitative mass spectral analysis of indole-3-acetic Acid in plants. , 1986, Plant physiology.

[43]  H. Kaldewey Transport and Other Modes of Movement of Hormones (Mainly Auxins) , 1984 .

[44]  A. Trewavas,et al.  Is plant development regulated by changes in the concentration of growth substances or by changes in the sensitivity to growth substances , 1983 .

[45]  K. Thimann,et al.  Hormonal factors controlling the initiation and development of lateral roots , 1980 .

[46]  B. Millard Quantitative mass spectrometry , 1978 .

[47]  J. Torrey,et al.  ROOT HORMONES AND PLANT GROWTH , 1976 .

[48]  T. Steeves,et al.  Patterns in plant development: Subject index , 1972 .

[49]  H. Schlenk,et al.  Esterification of Fatty Acids with Diazomethane on a Small Scale , 1960 .

[50]  D. D. Kosambi The estimation of map distances from recombination values. , 1943 .